Canonical Allele Identifier: CA1583107921

Gene: SLC22A4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132297674G= , CM000667.2:g.132297674G=	GRCh38
NC_000005.9:g.131633367G= , CM000667.1:g.131633367G=	GRCh37
NC_000005.8:g.131661266G=	NCBI36
NG_012129.1:g.8223G=
NG_012129.2:g.8223G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.393+2665G= MANE Select	ENSP00000200652.3:n.393+2665G=
ENST00000200652.3:c.393+2665G=	ENSP00000200652.3:n.393+2665G=
ENST00000491257.1:n.197+2053G=
NM_003059.2:c.393+2665G=	NP_003050.2:n.393+2665G=
XM_006714675.2:c.-32+2665G=	XP_006714738.1:n.-32+2665G=
XM_011543589.1:c.393+2665G=	XP_011541891.1:n.393+2665G=
XR_948289.1:n.1238+2053G=
XM_006714675.4:c.-32+2665G=	XP_006714738.1:n.-32+2665G=
XM_011543589.2:c.393+2665G=	XP_011541891.1:n.393+2665G=
XM_017009776.1:c.-136+2053G=	XP_016865265.1:n.-136+2053G=
NM_003059.3:c.393+2665G= MANE Select	NP_003050.2:n.393+2665G=